Canonical Allele Identifier: CA308817
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 202102
dbSNP Id: rs777518512

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665864C>T , CM000679.2:g.39665864C>T GRCh38
NC_000017.10:g.37822117C>T , CM000679.1:g.37822117C>T GRCh37
NC_000017.9:g.35075643C>T NCBI36
NG_008892.1:g.5519C>T , LRG_210:g.5519C>T
NG_042278.1:g.2884C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.259C>T MANE Select ENSP00000312624.2:p.Arg87Trp
ENST00000309889.2:c.259C>T ENSP00000312624.2:p.Arg87Trp
ENST00000578283.1:c.187C>T ENSP00000462787.1:p.Arg63Trp
NM_003673.3:c.259C>T , LRG_210t1:c.259C>T NP_003664.1:p.Arg87Trp
NM_003673.4:c.259C>T MANE Select NP_003664.1:p.Arg87Trp